Site Selective Concerted Nucleophilic Aromatic Substitutions of Azole-Ligated Diaryliodonium Salts

Бібліографічні деталі
Parent link:Advanced Synthesis and Catalysis
Vol. 365, iss. 4.— 2023.— [P. 535-543]
Співавтор: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Інші автори: Vlasenko Yu. A. Yuliya Aleksandrovna, Kuczmera T. Thomas, Antonkin N. S. Nikita Sergeevich, Valiev R. R. Rashid Rinatovich, Postnikov P. S. Pavel Sergeevich, Nachtsheim B. J. Boris
Резюме:Title screen
Diaryliodonium salts are electrophilic arylation reagents in transition metal-catalyzed and transition metal-free reaction methods. Herein we present the application of azole-stabilized diaryliodonium salts with additional thiophene-2-yl-ligands as substrates for metal-free nucleophilic arylations. Besides their synthesis, we demonstrate their application in chemoselective nitrations, oxygenations, aminations as well as thiolations under umpolung conditions. Convenient one-pot procedures based on their in situ formation are also discussed.
Опубліковано: 2023
Предмети:
Онлайн доступ:https://doi.org/10.1002/adsc.202201001
Формат: Електронний ресурс Частина з книги
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=669295
Опис
Резюме:Title screen
Diaryliodonium salts are electrophilic arylation reagents in transition metal-catalyzed and transition metal-free reaction methods. Herein we present the application of azole-stabilized diaryliodonium salts with additional thiophene-2-yl-ligands as substrates for metal-free nucleophilic arylations. Besides their synthesis, we demonstrate their application in chemoselective nitrations, oxygenations, aminations as well as thiolations under umpolung conditions. Convenient one-pot procedures based on their in situ formation are also discussed.
DOI:10.1002/adsc.202201001